A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997445



Internal ID21906788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37681578..37681702hg38UCSC Ensembl
chr4:37683200..37683324hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552918
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997445
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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